Canonical Allele Identifier: CA404246227

Gene: MAN2B1

Linked Data

• MyVariant Identifiers: chr19:g.12767793G>T (hg19) ; chr19:g.12656979G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12656979G>T , CM000681.2:g.12656979G>T	GRCh38
NC_000019.9:g.12767793G>T , CM000681.1:g.12767793G>T	GRCh37
NC_000019.8:g.12628793G>T	NCBI36
NG_008318.1:g.14799C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.1497C>A MANE Select	ENSP00000395473.2:p.Ser499Arg
ENST00000221363.8:c.1494C>A	ENSP00000221363.4:p.Ser498Arg
ENST00000433513.5:n.103C>A
ENST00000456935.6:c.1497C>A	ENSP00000395473.2:p.Ser499Arg
ENST00000466794.5:n.1396C>A
ENST00000495617.1:n.673C>A
ENST00000593686.1:c.107C>A
ENST00000595880.5:n.94C>A
NM_000528.3:c.1497C>A	NP_000519.2:p.Ser499Arg
NM_001173498.1:c.1494C>A	NP_001166969.1:p.Ser498Arg
XM_005259913.1:c.1500C>A	XP_005259970.1:p.Ser500Arg
XM_011528017.1:c.396C>A	XP_011526319.1:p.Ser132Arg
XM_005259913.2:c.1500C>A	XP_005259970.1:p.Ser500Arg
XM_024451518.1:c.396C>A	XP_024307286.1:p.Ser132Arg
NM_000528.4:c.1497C>A MANE Select	NP_000519.2:p.Ser499Arg
NM_001173498.2:c.1494C>A	NP_001166969.1:p.Ser498Arg